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Antioxidant activity of food proteins and food protein hydrolysates.

机译:食品蛋白质和食品蛋白质水解物的抗氧化活性。

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摘要

The objective of this research was to study the antioxidant activity of soybean protein hydrolysates (SPH) and chickpea protein hydrolysates (CPH) at different concentrations, and to measure the antioxidant activity of fractions collected from the RP-HPLC analysis of SPH and CPH. Protein hydrolysates were prepared by the proteolytic enzyme trypsin. The hydrolysates obtained were subjected to DPPH (1, 1-diphenyl-2 picrylhydrazyl) radical scavenging assay. The SPH and CPH at concentration of 2.5-10 mg/ml showed antioxidant activity of 16.5-32 % and 3.4-26.8 %. SPH and CPH were fractionated by using RP-HPLC on C18 column. The antioxidant activity of four SPH and CPH fractions (F I, F II, F III, and F IV) was measured by using DPPH radical scavenging assay. For SPH, antioxidant activity of F III (47.7 %) was higher than other fractions at protein concentration of 1 mg/mL and for CPH; F II showed maximum antioxidant activity 27.9 % at protein concentration 1 mg/mL. The results from the SDS-PAGE confirmed the hydrolysis of protein samples.;The second part of the study was to measure the impact of high pressure processing (HPP) on the degree of hydrolysis and antioxidant activity of proteins. High pressure processing (HPP) of isolated soybean protein (ISP) and isolated chickpea protein (ICP) was done at 400 MPa and 600 MPa for 5 min and 10 min. The degree of hydrolysis of isolated soybean protein and isolated chickpea protein treated with high pressure processing and with trypsin hydrolysis showed continuous increase from 12.4 to 24.9 % for SPH and 13.6 to 26.2 % for CPH. The DPPH radical scavenging assay showed a more than two fold increase in antioxidant activity of SPH and CPH: 67 % as compared to the 32 % of SPH without HPP and 56.6 % as compared to the 26.8 % of CPH without HPP at concentration 10 mg/mL. These results show that HPP increased the degree of hydrolysis and antioxidant activity of protein hydrolysates.
机译:本研究的目的是研究不同浓度的大豆蛋白水解物(SPH)和鹰嘴豆蛋白水解物(CPH)的抗氧化活性,并测量从SPH和CPH的RP-HPLC分析中收集的馏分的抗氧化活性。通过蛋白水解酶胰蛋白酶制备蛋白水解物。对获得的水解产物进行DPPH(1,1-二苯基-2甲基联苯甲基)自由基清除测定。 SPH和CPH的浓度为2.5-10 mg / ml,其抗氧化活性为16.5-32%和3.4-26.8%。通过在C18柱上使用RP-HPLC分离SPH和CPH。通过使用DPPH自由基清除测定法测量四个SPH和CPH馏分(FI,FIII,FIIII和FIV)的抗氧化活性。对于SPH,在蛋白质浓度为1 mg / mL和CPH下,F III的抗氧化活性(47.7%)高于其他组分。 F II在1 mg / mL的蛋白质浓度下显示最大抗氧化活性27.9%。 SDS-PAGE的结果证实了蛋白质样品的水解。研究的第二部分是测量高压处理(HPP)对蛋白质水解程度和抗氧化活性的影响。对分离的大豆蛋白(ISP)和分离的鹰嘴豆蛋白(ICP)进行高压处理(HPP),分别在400 MPa和600 MPa下进行5分钟和10分钟。经高压处理和胰蛋白酶水解处理的分离大豆蛋白和鹰嘴豆蛋白的水解度显示,SPH和CPH分别从12.4%增至24.9%和13.6%至26.2%。 DPPH自由基清除试验显示SPH和CPH的抗氧化活性提高了两倍以上:在浓度为10 mg / g时,无HPP的SPH为32%,而无HPP的CPH为26.8%,与之相比为32.6%。毫升这些结果表明,HPP增加了蛋白质水解产物的水解度和抗氧化活性。

著录项

  • 作者

    Singh, Prabhjot.;

  • 作者单位

    McGill University (Canada).;

  • 授予单位 McGill University (Canada).;
  • 学科 Agriculture Food Science and Technology.
  • 学位 M.Sc.
  • 年度 2011
  • 页码 90 p.
  • 总页数 90
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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